Scalable High Quality Aptamer Generation via Chemically-Augmented Particle Display

Information

  • Research Project
  • 9749438
  • ApplicationId
    9749438
  • Core Project Number
    R44GM123822
  • Full Project Number
    3R44GM123822-02S1
  • Serial Number
    123822
  • FOA Number
    PA-16-302
  • Sub Project Id
  • Project Start Date
    7/14/2017 - 7 years ago
  • Project End Date
    5/31/2020 - 4 years ago
  • Program Officer Name
    HAGAN, ANN A
  • Budget Start Date
    6/4/2018 - 6 years ago
  • Budget End Date
    5/31/2019 - 5 years ago
  • Fiscal Year
    2018
  • Support Year
    02
  • Suffix
    S1
  • Award Notice Date
    9/10/2018 - 6 years ago

Scalable High Quality Aptamer Generation via Chemically-Augmented Particle Display

ABSTRACT Nucleic acid aptamers have shown great promise as the synthetic alternative to monoclonal antibodies (mAbs) in therapeutics, diagnostics, and R&D tools1?7. Despite their key advantages of chemical and thermal stability, consistent quality8, sequenceability and amplifiability, aptamers are used far less widely than mAbs, primarily due to poor performance in real-life applications. The root of the aptamer performance problem lies in the limited chemical diversity offered by the 4 natural nucleic acid bases, in contrast to the 20 different amino acids composing antibody. Fortunately, as a synthetic scaffold, aptamers have the potential to incorporate a broad range of chemical diversity through use of modified nucleotides. However, due to fundamental limitations of selection-based discovery methods (SELEX), chemically modified aptamers are just beginning to scratch the surface, and have been largely limited to a single type of modification - deoxyuracil carrying hydrophobic functional groups. The potential of a broad range of modified bases for aptamer discovery and application is yet uncharted. We propose to develop Chemically-Augmented Particle Display (CAPD), a novel approach that enables us to discover modified aptamers with a broad range of chemical diversity that exhibit greatly improved affinity, specificity, stability in biological media and the capability serve as a viable alternative to antibodies in real-world applications. Our method has the potential to screen a wide range of distinct chemically modified aptamer libraries, wherein we measure the affinity and specificity of every aptamer candidate and explicitly isolate the highest performance binders with the best chemical modifications. In phase I, we will develop the CAPD platform and validate aptamers generated with it in standard ELISA assays in serum and compare to natural DNA aptamers and commercial mAbs. In phase II, we will then develop a production pipeline to create and validate an initial catalog of aptamer pairs to address unmet needs in the research and diagnostics markets. We will deliver aptamer pairs for no less than 30 priority targets (identified by our customers and healthcare stakeholders) for use in point of care diagnostics and research assays as which are severely underserved by antibodies. We will make all these aptamers immediately available for research and diagnostics markets. If successful, we believe CAPD will revolutionize aptamer discovery, and enable synthetic aptamers to achieve mainstream adoption in biomedical research, diagnostics and therapeutics.

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    R44
  • Administering IC
    GM
  • Application Type
    3
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    227400
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    859
  • Ed Inst. Type
  • Funding ICs
    NIGMS:227400\
  • Funding Mechanism
    SBIR-STTR RPGs
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    APTITUDE MEDICAL SYSTEMS, INC.
  • Organization Department
  • Organization DUNS
    078377924
  • Organization City
    SANTA BARBARA
  • Organization State
    CA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    931054321
  • Organization District
    UNITED STATES